Tool · 510(k)

510(k) Predicate Finder

Find potential predicate devices for your 510(k) submission. Enter a K-number to find all clearances with the same product code, a three-letter product code to browse clearances directly, or search by device name.

Product Code: LRK FDA class 2

Device, Anti-Snoring

Dental

View full classification →

The Anti-Snoring Device is a dental appliance designed to reposition the mandible or maintain airway patency during sleep to reduce or eliminate snoring, typically through oral repositioning mechanisms. It is classified as a Class 2 (moderate risk) device, subject to general and special controls, and requires 510(k) premarket notification. The product code is LRK, regulated under 21 CFR 872.5570, within the Dental medical specialty. This device is eligible for third-party review under the FDA's accredited persons program.

510(k) Clearances

50+ matches
K Number
Device Name
SleepRight Snore Aid
Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue
DNA Appliance
Hushd Pro Avera
EMA 3D
Difiney Anti Snoring Device
airVata™
Aniti-Snore Mouthguard+
C.A.R.E. Appliance (DNA, mRNA, mmRNA)
Silent Nite® Sleep Appliance with the Glidewell Hinge™ (SNGLHG)
The AVEOtsd (Tongue Stabilizing Device) Mouthpiece
ApneaRX Pro
Emerald Herbst
DNA Appliance
SilentZPro 2.0
SNOR LOCK
CUSTMBITE Snoring System
Soft Palate Elevator
ProSomnus EVO [PH] Sleep and Snore Device, ProSomnus EVO [PH] Sleep and Snore Device with Patient Monitoring
Soundly Anti Snoring Device
ZQuiet Advance
Respire Clear
Morpheus
Elevo Snoring Intervention Set
EndSnorZ Sleep Appliance
SmartGuard Anti-Snoring Device
mmRNA appliance
Snore Bandit
Silent Nite Sleep Appliance with the Glidewell Hinge
Serena Sleep Block Mandibular Advancement (BMA), Serena Sleep Elastic Mandibular Advancement (EMA)
Classic
Advanced Dental Appliance
NOA Sleep Apnea and Snoring Device
Vital Sleep
Somnos Anti-Snoring Mouth Guard
ProSomnus EVO Sleep and Snore Device, ProSomnus EVO Sleep and Snore Device with Patient Monitoring
Diamond Digital Sleep Orthotic (DDSO)
Respire Pink AT (Hard, Hard/Soft, EF)
MPowRx Snoring Solution (also known as Good Morning Snore Solution)
SleepTight Mouthpiece STZ
Sapphire Dorsal Comfort Fit
O2Vent Optima
Silent Nite sl
Twilite Appliance
TD Clip
SomnoDent Avant
PureSleep (OTC use)
ZAPnea Oral Appliance
Kava and Kava with Herbst
TrueDorsal Devices

What is a Predicate Device?

A predicate device is a legally marketed device that a new 510(k) applicant uses to demonstrate substantial equivalence. The FDA's 510(k) pathway requires manufacturers to show that their device has the same intended use and similar technological characteristics as one or more predicate devices already cleared for commercial distribution.

Finding the right predicate is a critical step in 510(k) strategy. Manufacturers typically search for cleared devices with the same FDA product code, which groups devices by their intended use and regulatory classification. This tool helps you identify potential predicates by browsing all clearances within a product code.

Note that predicate devices must be legally marketed — they cannot be devices that were cleared but never commercialized, or devices subject to a mandatory recall. The determination of substantial equivalence considers intended use, technological characteristics, and performance data.

Popular Product Codes

Commonly searched